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1 with the conjugate vaccine compared with the pneumococcal polysaccharide vaccine.
2 re due to serotypes covered by the 23-valent pneumococcal polysaccharide vaccine.
3 were serotypes represented in the 23-valent pneumococcal polysaccharide vaccine.
4 lysaccharides used to formulate a polyvalent pneumococcal polysaccharide vaccine.
5 ates were serotypes that are included in the pneumococcal polysaccharide vaccine.
6 9F, and 23F linked to CRM197, or a 23-valent pneumococcal polysaccharide vaccine.
7 f dementia compared to the control 23-valent pneumococcal polysaccharide vaccine.
8 polysaccharide antigens was assessed using a pneumococcal polysaccharide vaccine.
9 pneumonia following receipt of the 23-valent pneumococcal polysaccharide vaccine.
10 long-lasting, impaired antibody responses to pneumococcal polysaccharide vaccines.
11 the influence of Km and Gm allotype genes on pneumococcal polysaccharide vaccines.
12 ons manifest decreased antibody responses to pneumococcal polysaccharide vaccines.
14 7; Prevnar) in infancy followed by 23-valent pneumococcal polysaccharide vaccine (23vPPV; Pneumovax)
15 stem activation using the standard 23-valent pneumococcal polysaccharide vaccine, (3) daily sampling
16 -treated patients had decreased responses to pneumococcal polysaccharide vaccine (57% of patients had
17 uded in the 7-valent conjugate and 23-valent pneumococcal polysaccharide vaccines accounted for 78 pe
18 s, but it remains unclear whether use of the pneumococcal polysaccharide vaccine alters the overall r
21 rgeting high-risk groups was undertaken with pneumococcal polysaccharide vaccine, and subsequently ra
23 Four of 16 patients in group 1 responded to pneumococcal polysaccharide vaccine compared with 14 of
26 se findings support the effectiveness of the pneumococcal polysaccharide vaccine for the prevention o
29 e vaccine (PCV) followed by either a dose of pneumococcal polysaccharide vaccine or a fourth PCV dose
30 gate vaccine followed by 1 dose of 23-valent pneumococcal polysaccharide vaccine or a single dose of
31 rted that the 7-valent diphtheria-conjugated pneumococcal polysaccharide vaccine (PCV7) is safe and i
32 administration of the heptavalent conjugated pneumococcal polysaccharide vaccine (PCV7) were also ass
35 ther passive immunization with the 23-valent pneumococcal polysaccharide vaccine (Pneumovax(R) 23; PP
37 udy murine immune responses to the 23-valent pneumococcal polysaccharide vaccine Pnu-Imune, both in v
39 dose 6 months later, and 1 dose of 23-valent pneumococcal polysaccharide vaccine (PPSV23) 1 month lat
40 jugate vaccine (PCV13) followed by 23-valent pneumococcal polysaccharide vaccine (PPSV23) 2 months la
41 15-valent PCV (PCV15) followed by 23-valent pneumococcal polysaccharide vaccine (PPSV23) 8 weeks lat
42 gate vaccine (PCV13) compared with 23-valent pneumococcal polysaccharide vaccine (PPSV23) among US ad
43 ortions and incidence matching the 23-valent pneumococcal polysaccharide vaccine (PPSV23) and 13-vale
44 usly vaccinated with >/= 1 dose of 23-valent pneumococcal polysaccharide vaccine (PPSV23) and had CD4
45 rt 1 (n = 350) previously received 23-valent pneumococcal polysaccharide vaccine (PPSV23) and were ra
46 tion Practices has recommended the 23-valent pneumococcal polysaccharide vaccine (PPSV23) for nonelde
47 PD), with the effectiveness of the 23-valent pneumococcal polysaccharide vaccine (PPSV23) for prevent
49 te vaccine (PCV13) followed by the 23-valent pneumococcal polysaccharide vaccine (PPSV23) remains unc
51 Controversy persists over the benefits of pneumococcal polysaccharide vaccine (PPV) for adults at
55 umonia (n = 16) and healthy volunteers given pneumococcal polysaccharide vaccine (PPV; n = 14) or pne
56 (PCV13) concurrently, followed by 23-valent pneumococcal polysaccharide vaccine (PPV23) 2 months lat
57 determine the effectiveness of the 23-valent pneumococcal polysaccharide vaccine (PPV23) among Navajo
59 grouped serotypes contained in the 23-valent pneumococcal polysaccharide vaccine (PPV23) decreased at
63 >/= 200 randomized to receive the 23-valent pneumococcal polysaccharide vaccine (PPV23) or placebo a
64 V (PCV13) vs regions that used the 23-valent pneumococcal polysaccharide vaccine (PPV23) was also ana
65 65 years or older; previously only 23-valent pneumococcal polysaccharide vaccine (PPV23) was recommen
67 althy human adults with Pneumovax (23-valent pneumococcal polysaccharide vaccine [PPV23]), IgG anti-c
68 (PCV) followed by either a dose of 23-valent pneumococcal polysaccharide vaccine (PSV23) or a fourth
72 rs after transplantation and the response to pneumococcal polysaccharide vaccine was significantly lo
73 sera of people immunized with the 23-valent pneumococcal polysaccharide vaccine, we confirmed that h
74 ne response to that induced by the 23-valent pneumococcal polysaccharide vaccine, which has been the
75 eritoneal B1b compartment, immunization with pneumococcal polysaccharide vaccine yielded comparable a